WO2004089591A1

WO2004089591A1 - Molded article of reclaimed thermoplastic resin

Info

Publication number: WO2004089591A1
Application number: PCT/JP2004/004465
Authority: WO
Inventors: Yasuhiro Suzuki; Hidetoshi Oido
Original assignee: Suzuka Fuji Xerox Co., Ltd.; Tohpe Corporation
Priority date: 2003-04-01
Filing date: 2004-03-29
Publication date: 2004-10-21
Also published as: JPWO2004089591A1; US20060194891A1; JP3986536B2; EP1609573A1; EP1609573A4

Abstract

A reclaimed-thermoplastic-resin molding which is obtained by a method in which a coated molding comprising a molding consisting mainly of a thermoplastic resin and a coating material which consists mainly of a thermoplastic resin having compatibility with that thermoplastic resin and with which at least part of the molding is coated is pulverized without removing the coating film and then remolded, wherein the coating material contains a pigment which has been surface-treated with a resin having compatibility with the thermoplastic resin constituting the molding and with the thermoplastic resin constituting the coating material. Because of the pigment, the reclaimed-thermoplastic-resin molding can have intact material properties even when recycled.

Description

Recycled thermoplastic resin molded product

Technical field

TECHNICAL FIELD The present invention relates to a recycled thermoplastic resin molded product that is pulverized and remolded without separating or peeling off a coating film on the surface of a painted molded product.

Light

Background Art This is a case where molded products (painted products) made of thermoplastic resin with fine L coating film are recycled, and the vehicle of the paint (thermosetting or thermoplastic resin that constitutes the paint) is used for molding. If the resin has no compatibility (solubility), do not separate or peel off the paint film. If the product is recycled with the paint film applied, the paint resin undergoes phase separation in the process of heating and melting, and the recycled resin molded product It is known that the physical properties such as the strength of the polymer decrease.

For this reason, by using a paint that has compatibility (solubility) between the thermoplastic resin, which is the main component of the molded product, and the paint resin, which is the vehicle for the paint, it can be recycled without peeling off the paint film. (See, for example, Japanese Patent No. 328991).

However, in recent years, metallic paints, which have excellent design properties, are often applied to plastic housings of home appliances and OA equipment, and metallic paints, for example, are increasingly mixed with pigments such as aluminum flakes. Was. If a coated molded article coated with a paint containing such a pigment is recycled with the coated film, there is a problem that physical properties such as strength of the regenerated molded article are reduced.

The strength of the regenerated resin is such that the pigments such as aluminum flakes are incompatible (soluble) with the resin constituting the molded article and the resin constituting the paint, so the pigment is separated between the pigment and the resin of the molded article. However, this is the cause of the deterioration in physical properties.

The present invention has been made in order to solve the above problems, An object of the present invention is to provide a recycled thermoplastic resin molded product that is not affected by deterioration in physical properties, etc. due to a pigment mixed in a process in which a molded product recycled without separating or peeling off a coating film is ground and remolded. It is. Disclosure of the invention

The recycled thermoplastic resin molded product according to claim 1 is a molded product containing a thermoplastic resin as a main component, the thermoplastic resin having compatibility (solubility) with the thermoplastic resin as a main component. In a regenerated thermoplastic resin molded product that has been crushed and re-molded with the paint film applied to at least a part of the paint, with the coating still applied, the pigment is added to the paint. Since the surface is treated with a resin that has compatibility (solubility) with the thermoplastic resin forming the molded article and the thermoplastic resin forming the paint, even if the pigment is dispersed in the regenerated molded article, the Reduction can be suppressed.

Here, having compatibility (solubility) means that the thermoplastic resin, which is the main component of the molded article, and / or the thermoplastic resin, which constitutes the paint, and the resin coated on the surface of the pigment. In the heat-melting stage, the property that any one of them is melted and physically bonded by heat fusion, heat bonding, intermolecular force, anchor effect, diffusion, etc. Incompatibility (dissolution) can be confirmed by observing the presence or absence of peeling using a transmission electron microscope.

In addition to the above properties, the case where the respective resins are mixed at a molecular level is also included. The recycled thermoplastic resin molded product according to claim 2 is resin-coated because the pigment is an inorganic and / or organic compound in the recycled thermoplastic resin molded product according to claim 1. Thus, even if the pigment is dispersed in the regenerated molded article, it is possible to suppress a decrease in physical properties.

The recycled thermoplastic resin molded article according to claim 3 is a recycled thermoplastic resin molded article according to claim 1, wherein the pigment is aluminum flake, so that the pigment has excellent design. Even if the painted molded product coated with the brick paint is pulverized and remolded, the deterioration of the physical properties can be suppressed. The recycled thermoplastic resin molded product according to claim 4 is the recycled thermoplastic resin molded product according to claim 2 or 3, wherein the thermoplastic resin constituting the paint is thermoplastic acryl. Resin or styrene-modified acryl resin. Resin-coated aluminum flakes have compatibility (solubility) and can suppress deterioration of physical properties even when pigments are dispersed in regenerated molded articles.

The recycled thermoplastic resin molded article according to claim 5 is a recycled thermoplastic resin molded article according to claim 3, wherein the aluminum flakes are covered with an organic polymer. Even if a painted product coated with a highly-expensive metallic paint is pulverized and remolded, the deterioration in physical properties can be suppressed.

The recycled thermoplastic resin molded article according to claim 6 is a recycled thermoplastic resin molded article according to claim 5, in which the organic polymer is an acrylic resin, and thus has excellent design. Even if the molded product coated with the evening lick paint is crushed and remolded, the deterioration of physical properties can be suppressed.

The recycled thermoplastic resin molded product according to claim 7 is the recycled thermoplastic resin molded product according to claim 5, wherein the aluminum flakes dissolve an ethylenically unsaturated monomer in an organic solvent. By heat polymerization in the presence of a polymerization initiator, or by reacting at least two kinds selected from the group consisting of an oligomer having at least one polymerizable double bond and a monomer. Since it is covered with a polymer, it is possible to suppress a decrease in physical properties even when a molded article coated with a metallic paint having excellent design properties is pulverized and remolded.

The recycled thermoplastic resin molded article according to claim 8 is the recycled thermoplastic resin molded article according to claim 5, wherein the coating amount of the organic polymer covering the aluminum flakes is the same as that of the aluminum flakes. 5% by mass or more based on the mass, so that even if the painted molded product coated with the tallic paint is pulverized and re-molded, there is no separation between the pigment and the resin constituting the molded product. Physical properties can be prevented from deteriorating.

(The invention's effect) .

Pulverize and re-mold a coated molded product mainly composed of thermoplastic resin, with a coating Even if recycled, the pigment has compatibility (solubility), so that there is an effect that the physical properties, such as mechanical strength, of the regenerated thermoplastic resin molded article mixed with the coating film do not decrease. BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 is a perspective view showing an embodiment of a recycled thermoplastic resin molded product of the present invention. BEST MODE FOR CARRYING OUT THE INVENTION

Hereinafter, the present invention will be described in detail.

〔Thermoplastic resin〕

In the present invention, the type of the thermoplastic resin used as the material of the molded article is not particularly limited as long as it is a thermoplastic resin generally used for molding.

Examples of thermoplastic resins include polystyrene-based resins obtained by polymerizing styrene-based monomers, for example, polystyrene, high-impact polystyrene, nitrile-based monomers; styrene, which is a copolymer with styrene-based monomers Resin consisting of acrylonitrile-styrene copolymer, nitrile monomer-styrene monomer-butadiene rubber polymer, olefin rubber polymer, acrylic rubber polymer For example, styrene resins such as acrylonitrile butadiene, or ethylene rubber, or acrylyl rubber styrene copolymer (A83 and 83), polyethylene (PE), polypropylene (PP, including PP containing olefin rubber) ), Polyolefin resin (including PPE, modified PPE and modified PP e), polycarbonate Engineering plastics such as plastic (PC), polyamide (PA), polysulfone (PSF), polyetherimide (PE 1), and polymethyl methacrylate (PMMA); polyethylene terephthalate (PET); Examples include polyester resins such as PBT), vinyl resins such as vinyl chloride (PVC), and mixtures of two or more of the above thermoplastic resins.

Particularly useful as a material for a molded article used in the present invention is a polystyrene-based material. Resin, nitrile monomer スチレン copolymer with styrene monomer, PPE, ABS, AAS (ASA), AES, high impact polystyrene, or ABS and / or HI PS (including Hi PS) A mixture of PPE, PP, ABS and Z or HI PS (including Hi PS) with PC, PA, PBT, PS F. PEI, etc., a polymer blend, or a polymer alloy.

Hereinafter, some of the thermoplastic resins will be described in detail.

(A: Styrene resin)

The styrene-based resin to be used in the present invention is a resin containing at least 25% by mass or more of a styrene-based monomer in a polymer, and is a homopolymer of the styrene-based monomer or the styrene-based monomer. A copolymer of two or more of the following: a copolymer of the styrene-based monomer and one or more of other monomers copolymerizable with the styrene-based monomer; Rubber polymer such as styrene-based resin and gen-based rubber obtained by polymerizing sole or two or more of the above-mentioned styrene-based monomers (including HiPS) to an olefin-based or acryl-based rubber. And a polymer blend or a polymer blend.

Typical examples of the styrene resin include polystyrene (PS), which is a styrene homopolymer, the gen rubber polymer, the acrylic rubber polymer, and the olefin rubber polymer. Impact-resistant polystyrene, which is a blend polymer of styrene-grafted rubbery polymer obtained by graft polymerization of styrene and polystyrene {HI PS (PS containing graphene-based rubbery polymer), Hi PS, acrylonitrile-styrene copolymer Copolymer (AS), styrene-butadiene copolymer, styrene 'α-methylstyrene copolymer, styrene, maleic anhydride copolymer, styrene-methyl methacrylate copolymer, styrene-ethylene copolymer, styrene Acrylonitrile and styrene are added to ethylene-propylene-butadiene copolymer and AΒS resin in which acrylonitrile / styrene copolymer is blended with copolymerized graft rubber-like polymer, ACS, which is a mixed resin of chlorinated polyethylene and acrylonitrile / styrene copolymer, or olefin polymer Of acrylonitrile and styrene containing darafftolefin rubbery polymer grafted with acrylonitrile and styrene AES (AbS), which is a mixed resin of terpolymer and acrylonitrile-styrene copolymer, acrylonitrile containing acrylonitrile and styrene, which is obtained by graft polymerization of acrylonitrile and styrene onto acrylic rubbery polymer AAS {(ASA) (Ab S)}, which is a mixed resin of the terpolymer and acrylonitrile / styrene copolymer, acrylonitrile'dimethylsiloxane / styrene copolymer and acrylonitrile / butadiene / styrene copolymer resin A mixed resin of ASiS, an olefin polymer or a grafted olefin polymer containing styrene and a grafted olefin polymer obtained by graft-polymerizing styrene with a 7-carbon rubber polymer; Mixed resin of graft acryl-based rubber polymer and styrene polymer obtained by graft-polymerizing styrene with acryl-based rubber polymer (H i PS).

In the present invention, AAS, .. and AES are referred to as AbS, and a PS resin reinforced (blended) with a graft-olefin-based rubbery polymer and / or a graft-acrylic-based rubbery polymer is referred to as HiPS.

(B: Polyphenylene ether (PPE) resin)

A typical example of the PPE resin targeted by the present invention is poly (2,6-dimethyl-1,4-phenylene ether) obtained by oxidative polymerization of 2,6-xylenol with a copper catalyst. However, there are also copolymers of 2,6-dimethyl-1,4-phenylene ether and 2,3,6-trimethylylene 1,4-phenylene ether, and 2,6-dimethylphenol and 2,3 And 6-dorimethylphenol.

Further, the PPE-based resin of the present invention includes those obtained by modifying the PPE-based resin with a styrene-based resin and / or an amide-based resin. .

(C: polycarbonate resin)

In the present invention, the PC resin can be used alone as a thermoplastic resin for molding (mold), but is mainly used as a material which is mixed with the above-mentioned styrene-based resin or ΡΡΕ-based resin to form a polymer alloy or a polymer blend. Also used.

The PC resin (aromatic PC resin) is not particularly limited as long as it is a polycarbonate derived from an aromatic dihydroxy compound. Examples of the aromatic dihydroxy compound include 2,2-bis (4-hydroxyphenyl) propane (also referred to as bisphenol A), tetramethylbisphenol8, tetrabromobisphenolA, bis (4- Hydroxyphenyl) p-diisopropylpyrubenzene, hydroquinone, resorcinol, 4,4'-dihydroxydiphenyl, etc. can be used, but usually bis (4-hydroxyphenyl) alkane dihydroxy compound is used. Preferred are, in particular, bisphenol A or a combination of bisphenol A and another aromatic dihydroxy compound.

(D: polyolefin resin)

Polyolefin resin is a resin obtained by polymerizing one or more α-olefins using a radical initiator, a metal oxide catalyst, a Tiedlar-Natta catalyst, a Kaminsky catalyst, or the like. And two or more of the above resins may be mixed. The above-mentioned refining olefin is a linear / branched or cyclic olefin having a polymerizable double bond at the α-position, and usually has 2 to 8 carbon atoms. Specific examples of the olefin include ethylene and propylene. The polyolefin resin which is the subject of the present invention may be copolymerized with another monomer copolymerizable with α-lefin.

Other monomers include acrylic acid, methacrylic acid, maleic acid, itaconic acid, methyl acrylate, ethyl acrylate, methyl methacrylate, maleic anhydride, aryl maleic imide, alkyl maleic imide, etc. Unsaturated organic acids or derivatives thereof; vinyl esters such as vinyl acetate and vinyl butyrate; aromatic pinyl compounds such as styrene and methyl styrene; vinyl trimethyl methoxy silane; 1,4-hexadiene, 4-methyl-1,4-hexadiene, 5-4-methyl_1,4-hexadiene, dicyclopentene, ethylidene norbornene (4-ethylidene_2) A small amount of a non-conjugated diene such as non-porene) may be copolymerized. Typical examples of the polyolefin-based resin include polyethylene, polypropylene, ethylene-vinyl acetate copolymer, and ethylene-acrylic acid copolymer. The polyolefin-based resin is used as a molding material alone or in the form of a mixture of two or more kinds. It may be mixed with other thermoplastic resins such as S, HI PS and Hi PS, AS, 883 and 83, PPE (including modified PPe) resin.

(Polymer blend, polymer alloy)

The thermoplastic resin may be a polymer blend or a polymer alloy by mixing two or more kinds. The polymer blend or polymer alloy is produced by, for example, screw kneading in an extruder. Further, in order to impart mechanical properties to the thermoplastic resin for molding, the gen-based rubber polymer, the olefin rubber-based polymer, the acryl-based rubber-based polymer, etc. , SBR, STR, IR, CR, CBR, IBR, IBBR, IIR, acrylic rubber, polysulfide rubber, urethane rubber, polyether rubber, epichlorohydrin rubber, chlorobutyl rubber, hydrogenated nitrile rubber, fluoro rubber, etc. Other thermoplastic resins such as rubbers, ethylene-vinyl acetate copolymers, acrylic resins, ethylene-ethyl acrylate copolymers, vinyl resins represented by vinyl chloride, and vorinol polyene may be mixed.

These rubbery polymers have compatibility (solubility) by block, random and graft copolymerization of the resin monomer to be compounded, if necessary. Considering the adhesion of the coating, a darafft copolymer is desirable. The graft polymer used in the present invention is a graft polymer whose trunk portion is a gen-based rubber polymer, an olefin-based rubber polymer, or an acrylic rubber polymer. A graft rubber that is a polymer and has a graft chain compatible with the thermoplastic resin used as a vehicle for the molded articles, accessory members, coating materials, printing inks and adhesives, welding rods, etc. It is a polymer.

That is, the rubbery polymer (rubber-like substance) used in the present invention includes a graft gen-based rubbery polymer (a gen-based rubber graft polymer), a graft olefin-based rubbery polymer (an olefin-based rubber graft polymer). ) And a grafted acrylic rubbery polymer (acrylic rubber graft polymer). In particular, an oligomeric rubber graft polymer and an acryl-based rubber daraft polymer which are excellent in thermal stability are preferred.

Hereinafter, each rubber-like (quality) substance (polymer) will be described.

(A: Grafted rubber polymer) As the gen-based rubbery polymer (gen-based rubber) which is a constituent component of the copolymer used in the present invention, a polymer or a copolymer containing conjugated gen as a main component is preferable. Of these, the content of the conjugated gen is preferably at least 75% by mass, particularly preferably at least 85% by mass. Specifically, polybutadiene, styrene-butadiene copolymer, acrylonitrile-butene diene copolymer, butyl butadiene acrylate copolymer, isoprene rubber, or the like can be used.

(B: Graftolefin rubbery polymer)

The olefinic rubbery polymer (olefinic rubber) used in the present invention can be copolymerized with one or more polymers of α-olefin, or one or more of the Q! -Olefins. It is a copolymer of one or more other monomers, especially a copolymer of ethylene and one or more other olefins, or another monomer copolymerizable therewith. , Especially copolymers with non-conjugated diene compounds. In the ethylene-olefin copolymer, the term “olefin” used as a monomer to be copolymerized with ethylene refers to α-olefin having 3 to 12 carbon atoms, specifically, propylene, Butene-1, 4-methylpentene-1, hexene-1, octene-1 and the like.

Examples of the non-conjugated diene compound include dicyclopentadiene, tricyclopentadiene, 5-methyl-2,5-norpolnadiene, 5-methylene-12-norpolene, 5-vinyl-2-norpolene, 5-ethylidene-2-diene. Norportene, 5 isopropylidene 2-norpolene, 5-isopropylidene-2-norpolene, 5- (1-butenyl) 1-2-norpolene, 5- (2-propenyl) 1-2-norporene, 5- (5 —Hexenyl) —2-norporene, 4,7,8,9-tetrahydroindene, and isopropylidenetetrahydroindindene, cyctooctane, vinylcyclohexene, 1,5,9-cyclododecattoluene, 6-methyl- 4,7,8,9-tetrahydroindene, 2,2'-dicyclopentenyl, trans-1,2-divinylcyclo 1,4-hexadiene, 2-methyl-1,4-hexadiene, 1,6-one-year-old kutadiene, 1,7-octadiene, 1,8-nonadiene, 1,9-decadiene, 3,6-dimethyl_1, 7-year-old, 4,5-dimethyl-1,7-octadiene, 1, 4, 7-octytriene, 5-methyl-1,8-nonagen, and the like.

Preferred among these non-covalent compounds are 5-ethylidene-2-norbornene (ENB) and / or dicyclopentene (DCP), more preferably dicyclopentene. A mixed resin of a graft olefin rubbery polymer using 5-ethylidene-2-norbornene and AS or PS improves the appearance of a molded article. In addition, the impact strength of the thermoplastic resin for molding can be increased by using EPDM as the rubbery polymer which is the main component of the graftolefin-based rubbery polymer rather than EPM.

The proportion of the ethylene monoolefin and the non-conjugated gen compound used as needed in the graft-olefin rubbery polymer used in the present invention is preferably ethylene / α- Olefin Z non-conjugated diene compound = 0.2 to 1.0 / 0.2 to 0.8 to 0.2, more preferably 0.5 to 0.9 / 0.25 to 0.75 / 0-0 , 1, and the molar ratio of ethylene / propylene is 60/40 or more, preferably 65/35 or more, that is, the reproducibility of the mechanical properties (impact resistance etc.) In view of the properties, it is desirable to use ethylene-propylene copolymer rubber (ΕΡΜ) or ethylene-propylene-non-conjugated gen compound terpolymer rubber (ΕΡ DM).

Further, the ethylene-α-branched olefin copolymer used in the present invention has a good Mooney viscosity (ML 1 + 4, 10 O) in view of reproducibility (heat stability, that is, recyclability). It is preferably 5 to 150, more preferably 10 to 120, and the optimal value is 20 to 80.

Representative examples of the above-mentioned rubber-based polymer are ethylene-propylene copolymer rubber (EPM), ethylene-propylene-non-conjugated gen compound terpolymer rubber (EPDM), ethylene-butene copolymer rubber (EBM) ), Ethylene / butene / non-conjugated gen compound terpolymer rubber (EBDM). The non-conjugated diene compound used in the EBDM is the same as that in the above-described EPDM.

(C: Graft acrylic rubbery polymer)

The acrylic rubbery polymer (acrylic rubber) used in the present invention is Desirable compounds such as acrylate, n-butyl acrylate, 2-ethylhexyl acrylate and the like are homopolymers of an acrylate having an alkyl group having 2 to 8 carbon atoms, or a copolymer of two or more of the above acrylates. Polymers or one or more of the above acrylates and non-conjugated gen compounds similar to those used in benzene or EPDM, acrylonitrile, methyl methacrylate, vinyl acetate, styrene, ethylene, propylene, etc. Copolymers with one or more other monomers, further functional monomers such as acrylic acid, methacrylic acid, / 3-hydroxyethyl methacrylate, acrylamide dimethylaminoethyl methacrylate, Alternatively, methacryloxypropyl trimethoxysilane, vinyl triacetoxysilane, p_ triethoxysilylsty Len, ρ-triethoxysilylstyrene, p-trimethoxysilyl-α-methylstyrene, ρ-triethoxysilyl-α-methylstyrene, acryloxypropyltrimethoxysilane, vinyltrimethoxysilane, Ν-β ( (Vinylbenzylaminoethyl-1-aminopropyl) A copolymer with a polymerizable silane coupling agent such as trimethoxysilane hydrochloride.

Examples of general-purpose acrylic rubbery polymers include, for example, boroethyl acrylate, poly η-butyl acrylate, η-butyl acryleyl acrylonitrile copolymer obtained by copolymerizing some of the above functional monomers. , Η-butyl acrylate-butene gen copolymer, η-butyl acrylate copolymer, η-butyl acrylate copolymer, η-butyl acrylate copolymer, η-butyl acrylate A preferred acrylic rubber, such as a vinyltrimethoxysilane copolymer, is an η-butyl acrylate-butadiene copolymer having a molar ratio of η-butyl acrylate / butadiene of 30/70 or more. The acryl-based rubbery polymer is usually produced by suspension polymerization, emulsion polymerization or the like. The average particle size of each of these rubbery polymer latexes of the gen type, the refining type and the acryl type must be in the range of 0.1 to 50 m, especially in the range of 0.15 to 15 xm. Is preferred. Here, when the average particle diameter of the gen-based rubbery polymer latex is less than 0.1 m, the impact resistance of the resin composition is poor, and when the average particle diameter exceeds 50 m, the surface gloss is reduced and satisfactory. Resin composition Can not get.

Regarding the gel content of the rubbery polymer latex of each of the gen-based, olefin-based, and acryl-based, it is preferably 40% by mass or more in consideration of the surface gloss and impact resistance of the obtained composition. Is 60% by mass or more. Here, the gel content refers to the mass fraction of the toluene-insoluble component after coagulating and drying the rubber latex.

As a method for producing these rubbery polymer latexes, an ordinary emulsion polymerization method can be employed. The average particle size, particle size distribution, and gel content can be set to desired ranges by carefully controlling the amount of polymerization water, emulsifier, chain transfer agent, polymerization temperature, stirring speed, and polymerization time during polymerization. It becomes possible.

(Graft copolymerization)

For the purpose of imparting compatibility (solubility) when the resin to be compounded is PS, styrene and a-alkyl monovinylidene are used as the aromatic vinyl monomers to be graft polymerized (copolymerized) with the rubbery polymer. Aromatic monomers (eg, a-methylstyrene, a-ethylstyrene, —methylvinyltoluene, a-methyldialkylstyrene, etc.), ring-substituted alkylstyrenes (eg, o, m, or p-vinyltoluene, o-ethylstyrene, p-Ethylstyrene, 2,4-dimethylstyrene, p_tertiarybutylstyrene, etc., ring-substituted halostyrene (eg, o-chlorostyrene, p-chlorostyrene, o-bromostyrene, 2,4-dichlorostyrene, etc.) ), Cyclic alkyl, cyclic halo-substituted styrene (for example, 2-methyl-1-methylstyrene, 2,6-dichlorostyrene, etc.) pinylnaphthalene, vinyl While styrene monomer such as anthracene and the like, are particularly styrene is preferable. These may be used alone or in combination of two or more. Generally, the alkyl substituent has from 1 to 4 carbon atoms and includes both linear and branched alkyl groups. If the resin to be compounded is AS, the styrene monomer and the vinyl cyanide monomer are grafted. Examples of the vinyl cyanide monomer include acrylonitrile, methacrylonitrile, ethacrylonitrile, fumaronitrile, and the like, and acrylonitrile is particularly preferable. These may be used alone or in combination of two or more.

Even if other monomers besides the styrene monomer and nitrile monomer are copolymerized. Good. The other monomer (third component) is not particularly limited as long as it is a monomer copolymerizable with the above styrene monomer and nitrile monomer, but is generally methyl (meth) acrylate. (Meth) acrylates such as methyl (meth) acrylate, N-phenylmaleimide, maleimide, N-methylmaleimide, N-ethylmaleimide, (p-bromophenyl) maleimide methacrylate, and hexylmaleimide Examples include unsaturated imides such as maleimides, maleic anhydride, and methacrylonitrile, and ril compounds.

As (meth) acrylates, alkyl esters having 1 to 4 carbon atoms, particularly methacrylates, are desirable. Here, the graft polymer (graft rubbery polymer) of the present invention is based on 65 to 85 parts by mass, preferably 70 to 80 parts by mass, of the monomer mixture 1 It is obtained by graft polymerization of 5 to 35 parts by mass, preferably 20 to 30 parts by mass. If the amount of the rubbery polymer exceeds 85 parts by mass, it becomes difficult to obtain good physical properties of the thermoplastic resin due to a relative decrease in a monomer to be grafted. Here, the proportion of the aromatic vinyl monomer is 50 to 99% by mass, preferably 60 to 90% by mass, and more preferably 70 to 80% by mass based on all the monomers to be grafted. %, And less than 50% by mass is not preferable because the dispersion state of the rubbery polymer in the thermoplastic resin is deteriorated. When the resin to be blended is AS, the proportion of the vinyl cyanide monomer is 1 to 50% by mass, preferably 10 to 40% by mass, more preferably 20 to 40% by mass based on all the monomers. ~ 30% by mass. If the other vinyl monomer copolymerizable therewith is used at 50% by mass or less, the object of the present invention can be achieved.

There are no particular restrictions on the production method of the graft polymer. Generally, the above monomers are graft-polymerized to a rubbery polymer obtained by generally known solution polymerization, emulsion polymerization, suspension polymerization, bulk polymerization, or the like. In general, a polymerization method is used in which the above-mentioned monomer is polymerized by the above-mentioned oil-soluble or water-soluble initiator and / or ultraviolet rays, or a high energy ray such as an electron beam in the presence of the above-mentioned olefin polymer. General polymerization methods such as bulk polymerization, suspension polymerization, solution polymerization, and emulsion polymerization are applied.

The graft rubbery polymer obtained by the graft polymerization contains, as a main component, a graft polymer in a narrow sense having a rubbery polymer as a trunk and a polymer chain of the above monomer as a branch. In a narrow sense, a rubbery polymer and / or a polymer comprising the above monomer is microblended with a graft rubbery polymer.

Various methods can be adopted as a method for adding components such as a monomer mixture, an emulsifier, a polymerization initiator, and a chain transfer agent in the graft polymerization. That is, a method of adding the whole amount at the initial stage of polymerization, a method of adding a part at the initial stage and continuously adding the rest, a method of continuously adding the whole amount, a method of adding twice or more, and the like are included.

There are no particular restrictions on the types of emulsifiers, polymerization initiators and chain transfer agents used, and reagents used in normal emulsion polymerization can be used. Typical emulsifiers include potassium rosinate, potassium stearate and potassium oleate, and polymerization initiators include organic hydroxide peroxide and a combination of sugar-containing pyrophosphate and ferrous sulfate and superacid salts. However, examples of the chain transfer agent include alkylthiol compounds S.

? The graft rubbery polymer obtained by L-polymerization is composed of an aromatic vinyl monomer, a vinyl cyanide monomer, and other vinyl monomers copolymerizable with these, in addition to the rubber polymer. It is a composition comprising a graft rubber component obtained by graft polymerization of a monomer and a non-daraft polymer component that does not graft onto a rubbery polymer. At this time, the graft ratio of the graft rubber component (mass ratio of the grafted polymer component to the rubbery polymer) is at least 10%, preferably at least 15%. Within this range, the compatibility (solubility) of the graft rubber polymer with the thermoplastic resin and the effect of improving the reproducibility of the thermoplastic resin, that is, the effect of preventing the reduction of the impact resistance during recycling, are balanced. . If the grafting ratio is less than 10%, the impact resistance of the resin composition and the surface appearance characteristics of the molded product are undesirably deteriorated. The mass ratio of the non-graft polymer component to the graft polymer is 5% by mass or more, preferably 8% by mass or more. If the amount of the non-graft polymer component is less than 5% by mass, aggregates appear on the surface of the molded article of the resin composition, and the appearance is significantly reduced, and the physical properties such as impact resistance are also unfavorably reduced. Further, the intrinsic viscosity of the non-grafted polymer component measured with a methyl ethyl ketone solvent, 30 is 0.3 dlZg or less, preferably 0.05 to 0.28 dlZg, more preferably 0.1 dlZg. 1-0.26 dl Zg. When the intrinsic viscosity exceeds 0.3 dl / g, the rubber particles are not uniformly dispersed in the matrix, and the impact resistance and the surface appearance characteristics are deteriorated. Not preferred. Here, it is generally considered that the degree of polymerization of the non-grafted polymer component and the grafted polymer component are almost the same, so if the chain length of the grafted polymer component is long, another rubber Entanglement with the polymer component grafted on the porous polymer Graph 1, preventing uniform dispersion of the rubber causes the deterioration of impact resistance and surface appearance characteristics. Graft ratio and intrinsic viscosity of non-grafted polymer should be adjusted by adjusting the ratio of rubbery polymer and monomer mixture, type and amount of polymerization initiator, type and amount of chain transfer agent, and type and amount of emulsifier. Can be controlled by

Hereinafter, the graft rubber polymer composed of a rubber polymer suitable for each thermoplastic resin will be described.

(1) Graft rubbery polymer for styrene resin

For styrenic resins, especially PS (or HIPS and HiPS), styrene and Z or other styrenes exemplified in the above (A: styrenic resin) as monomers similar to styrene Graft rubber polymer obtained by graft-polymerizing one or more of these monomers (such as styrene, olefin, or acrylic rubber polymer-containing styrene and monomers similar to Z or styrene). A styrene graft rubbery polymer which is a graft copolymer) is used.

Since the styrene graft rubbery polymer has a branched polymer chain of the styrene resin, particularly a styrene monomer having almost the same solubility parameter as PS,

Shows good compatibility (solubility) with PS.

For styrenic resins, especially AS (or ABS and AbS), one or more of styrene (styrene) and / or other styrenic monomers and acrylonitrile (cyanide) (Vinyl) and / or another graftile rubber polymer obtained by graft polymerization of one or more nitrile monomers (styrene and / or olefin and / or acryl rubber polymer containing styrene and / or A styrene nitrile-grafted rubbery polymer which is a graft copolymer of another styrene monomer or a monomer similar to styrene with acrylonitrile and / or another nitrile monomer is used. You.

In addition to the above-mentioned monomers, other monomers copolymerizable with the above-mentioned monomers are added to the rubbery polymer. Ft copolymerization. Such a monomer is exemplified in the section of (A: styrene resin).

Since the styrene nitrile graft olefin graft polymer has a styrene / nitrile copolymer chain having almost the same solubility parameter as the styrene resin, particularly AS (or ABS or AbS), it is a branch. Shows good compatibility (solubility) with AS (or ABS or AbS).

(2) Graft rubbery polymer for PPE resin

PPE is composed of a structural unit having a phenyl group as described above, and therefore, it is desirable that a styrene-grafted rubbery polymer be selected as the grafted rubbery polymer. Since the graft rubbery polymer has a styrene polymer chain having a similarity of solubility to PPE as a branch and has good compatibility (solubility) with the PPE resin, the graft rubbery polymer The polymer is stably mixed with the PPE resin without causing separation, and imparts the physical properties of the PPE resin.

(3) Rubbery polymer for olefin resin

For polyolefin-based resins such as polyethylene and polypropylene, the olefin-based rubbery polymer is substantially the same as the polyolefin-based resin, especially PP, because the same or similar monomer is copolymerized with the polyolefin-based resin. It has good solubility and good solubility, so it can be used as it is.

The use ratio of ethylene-α-olefin as a rubbery polymer for a refining-based resin and the non-conjugated gen compound used as necessary is preferably in terms of a mole fraction, and is preferably ethylene (θ !!-olefin). Non-conjugated diene compound = 0.2 to 1.0 / 0.2 to 0.8 / 0 to 0.2, more preferably 0.5 to 0.9 / 0.25 to 0.75 / 0-0 And the molar ratio of ethylene / propylene is at least 60/40, preferably at least 65/35. That is, the reproducibility (hereinafter, reproducibility) of the mechanical properties (impact resistance etc.) of the obtained resin molded product is From the point of view, it is desirable to use ethylene-rich ΕΡΜ or EPDM.

In addition, the ethylene viscosity of the ethylene-α-refined copolymer used in the present invention (ML 1 + 4, 100 ° C) is preferably from 5 to 150, more preferably from the viewpoint of reproducibility. In other words, 10 to 120, the optimal value is 20 to 80.

Further, in order to improve the impact resistance of the thermoplastic resin, a thermoplastic elastomer (TPE) may be added. The thermoplastic elastomer has properties of a vulcanized rubber at room temperature, but is thermoplastic and thermoformable, and is composed of a hard segment and a soft segment. Examples of the TPE include urethane-based elastomers, styrene-based elastomers, vinyl-based elastomers, and ester-based elastomers. [Mold (mold) object]

The molded article of the present invention is manufactured by using the above thermoplastic resin as a material by various molding methods such as injection molding, blow molding, vacuum molding, air pressure molding, press molding, extrusion molding, etc., and has a container shape, a box shape, a tray shape, It may have various shapes such as a sheet shape.

(Attached members)

The accessory member is manufactured using a thermoplastic resin having compatibility (solubility) with the thermoplastic resin of the above-mentioned molded article as a material by a molding method similar to that for the molded article. Attached members are, for example, handles, legs, seals and labels, frames, etc., which are adhered to the molded product.

The thermoplastic resin having compatibility (solubility) with the thermoplastic resin of a molded article refers to a thermoplastic resin which does not cause phase separation with the thermoplastic resin of the molded article even when heated and mixed and melted.

As the thermoplastic resin used for the accessory member, generally, a thermoplastic resin exemplified as the thermoplastic resin for the molded article is used. For example, when the thermoplastic resin of the above molded article is HIPS or HiPS or PS, the thermoplastic resin of the accessory member has compatibility (solubility) with the thermoplastic resin of the molded article. HI PS, Hi PS, PS etc. are used.

When the thermoplastic resin of the molded article is ABS, AbS or AS, the thermoplastic resin of the accessory member is ABS, AbS, AS, which has compatibility (solubility) with the thermoplastic resin of the molded article. ACS, AS i S, etc. are used.

When the thermoplastic resin of the molded article is PPE (or modified PPE), the thermoplastic resin of the accessory member is PPE, modified PPE, PS which has compatibility (solubility) with the thermoplastic resin of the molded article. , HI PS, Hi PS and the like are used. When the thermoplastic resin of the molded article is a mixture of PC / ABS or AbS (including polymer alloys and polymer blends; hereinafter, a mixture of PC / ABS, etc.), the thermoplastic resin of the accessory member is as follows: AS, AbS, ACS, ASiS, etc., such as a mixture of PC / ABS or AbS, which have compatibility (solubility) with the thermoplastic resin of the molded article, are used.

When the thermoplastic resin of the molded article is PP, the thermoplastic resin of the accessory member is halogenated, such as PP or chlorinated PP, which has compatibility (solubility) with the thermoplastic resin of the molded article. PP or the like is used.

(Coating material)

The coating material used in the present invention is to be applied to the surface of a molded article such as paint or ink, and a thermoplastic resin having compatibility (solubility) with the thermoplastic resin of the molded article is used as a vehicle. And That is, the thermoplastic resin as the vehicle is a resin that does not cause phase separation when melt-mixed with the thermoplastic resin of the molded article. Examples of such a concept include a styrene-based resin, a styrene-modified acryl resin, and the like for a molded article made of a styrene-based resin, a PPE resin, and a PC resin, and a polyolefin resin as a material. For molded articles, there are halogenated olefin resins and the like. The form of the coating material includes a solvent type, an emulsion type, a suspension type, a water-soluble type, and a powder. A fibrous derivative is added to the thermoplastic resin as the vehicle in order to improve coating workability, pigment dispersibility, drying property, and the like. Examples of such a fibrous derivative include methyl cellulose, ethyl cellulose, and the like. Examples include hydroxycellulose, hydroxypropylmethylcellulose, hydroxymethylmethylcellulose, cellulose acetate, benzylcellulose, nitrocellulose, and cellulose acetate butyrate. The viscosity of the cellulose acetate petitate is preferably in the range of 0.01 to 20 seconds. The acetyl group content of the cellulose acetate topylate is desirably in the range of 0 to 15.0%. The content of butyl groups in the cellulose acetate butyrate is preferably in the range of 30.0 to 55.0%.

The cellulose acetate is a diacetate cell orifice and has an oxidation degree of 50 to 60%, preferably 54 to 56%. The ethoxy group content of the ethyl cellulose is 4 It is desirable to be within the range of 5 to 50%. It is desirable that the methoxy group content of the methylcellulose is in the range of 19 to 31.5%. It is desirable that the hydroxypropoxy group content of the hydroxypropylmethylcellulose is in the range of 4 to 12%. The hydroxyethyl methylcellulose preferably has a hydroxyethoxy group content in the range of 4 to 12%. It is desirable that the viscosity of a 2% by mass aqueous solution of the hydroxyethyl cellulose is in the range of 20 to 1000 cps (mPa · s). Nitrocellulose © The nitrogen content is desirably 3% by mass or more.

The coating material may be a non-yellowing clear lacquer, but for coloring purposes, for example, pigments such as titanium white, chrome yellow, red iron, cobalt blue, carbon black, disperse dyes, cationic dyes, Dyes such as basic dyes, acid dyes, metal complex dyes, reactive dyes, direct dyes, sulfur dyes, vat dyes, IZOC dyes, and complex dyes are added. Further, a plasticizer such as dimethyl phthalate, dibutyl phthalate or octyl phthalate, an antioxidant, an ultraviolet absorber, a pigment or dye dispersant, or the like may be added to the coating material.

In particular, it is desirable to use a styrene-modified acrylic resin as a vehicle of a coating material used for a styrene resin, a PPE resin, and a PC resin.

The styrene-modified acryl resin is a copolymer composed of styrene and acryl ester. Examples of the acryl ester include methyl acrylate, ethyl acrylate, n-propyl acrylate, iso-propyl acrylate, n-butyl acrylate, iso-butyl acrylate, t-butyl acrylate, and 2-butyl acrylate. Examples include acrylates such as ethylhexyl acrylate, cyclohexyl acrylate, and tetrahydrofurfuryl acrylate, and methyl methacrylate, ethyl methacrylate, n-propyl methacrylate, iso-propyl methacrylate, n-butyl methacrylate, Methacrylates such as iso-butyl methacrylate, 2-ethylhexyl methacrylate, cyclohexyl methacrylate, tetrahydrofurfuryl methacrylate, stearyl methacrylate, lauryl methacrylate may be used. No.

The styrene-modified acrylic resin is compatible (soluble) with a thermoplastic resin such as a molded product. To the extent that the properties are not impaired, vinyl ethers such as methyl vinyl ether, ethyl vinyl ether, n-propyl vinyl ether, n-butyl vinyl ether, iso-butyl vinyl ether, nitrile monomers such as acrylonitrile and methacrylonitrile, and acetic acid Aliphatic vinyls such as vinyl and vinyl propionate, olefins such as ethylene and propylene, gens such as isoprene, chloroprene and butadiene, acrylic acid, methacrylic acid, itaconic acid, maleic acid, crotonic acid, atropic acid, citracone Α, such as acids,) 3-unsaturated carboxylic acids, 2-hydroxyethyl methacrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl methacrylate, 2-hydroxypropyl acrylate, hydroxyl groups such as aryl alcohol Monomers, amides such as acrylamide, methacrylamide, and diacetone acrylamide; amino group-containing monomers such as dimethylaminomethyl methacrylate, dimethylaminoethyl methacrylate, and dimethylaminopropyl acrylate; dalicidyl Epoxy group-containing monomers such as acrylate, daricidyl methacrylate, and glycidylaryl ether, methacryloxypropyltrimethoxysilane, vinylacetoxysilane, p-trimethoxysilylstyrene, P-triethoxysilylstyrene, P-trimethoxysilyl-Q! -Methylstyrene, p-triethoxysilyl-α-methylstyrene, acryloxypropyltrimethoxysilane, vinyltrimethoxysilane, Ν-3 Ν—Pierbenzilaminoethyl-amino-pro Pill) A monomer such as a vinyl monomer having a hydrolyzable silyl group such as trimethoxysilane 'hydrochloride may be copolymerized. The above monomers may be used alone or in combination of two or more.

Coatings and the like made of the styrene-modified acryl resin include the above-mentioned styrene-based resins (HIPS, HiPS, PS, ABS, AbS, AS), PPE (modified PPE), PC / ABS, AbS, HIPS, HiPS. It can be used in the coating of any molded article or the like composed of a mixture of the above, and has particularly good adhesion, weather resistance and workability, and is a particularly useful paint.

As a method of applying the above-mentioned molded article and the attached molded article using the paint or the like, any of known coating methods can be used, and generally, air spray coating is used.

Molding applied by painting or printing with the paint or ink used as the coating material Since the resin of the coating material is composed of a resin having compatibility (solubility) with the resin of the molded product, when such a molded product is recycled, the coating film and the like are separated from the molded product. There is no need to do this. Therefore, the resin molded product coated with the coating material of the present invention is a resin molded product having excellent recyclability.

(Colorant)

Materials to be incorporated into paints for decorative coloring purposes are called colorants, and pigments are usually used. Here, the pigment refers to a powder having a color insoluble in water or a solvent, or a powder having a color soluble in water. Examples of these are:

Among the inorganic pigments, white pigments include titanium oxide, zinc white, lead white, lithopone, barite, precipitated barium sulfate, calcium carbonate, gypsum, precipitated silica, and the like. Lamp black, titanium black, synthetic iron black, waste toner for copiers, etc. The gray pigments include zinc powder, lead suboxide, slate powder, etc., the white pigments include zinc white, antimony white, monobasic lead sulfate, lead white, titanium white, etc., and the black pigments include carbon black, There are lamp black, bone black, graphite, iron black and waste toner. In addition, red pigments include cadmium red, cadmium mercury red, silver vermilion, red ash, molybdenum red, lead red; kotan, chrome vermilion, red porcelain, lake red 4R, carmine FB, dinitroaniline orange, and pyrazolone orange. , Pyrazolone red, perinone orange, permanent red 2B, rake red R, bommaroonlight, pordo 10B, pommarmedium, choindigopordo, pommarou L, perylene vermilion, perilet power, perylene And benzimidazolone orange. Examples of the brown pigment include amber, iron oxide tea, cadmium yellow and the like. In addition, examples of yellow pigments include zinc yellow, loess; orcs and senna; yellow iron oxide: synthetic ocher, graphite, titanium yellow and the like. Green pigments include chromium oxide, cobalt green, chrome green, etc., graphite, yellow iron oxide, titanium yellow, loess, antimony yellow, barium yellow, monoazo pigments, disazo pigments, condensed azo pigments, isoindolinone face Pigments and slender pigments. Examples of the green pigment include chrome green, cobalt daline, chromium oxide, cyanine green, brominated green, and chrome green. Examples of blue pigments include ultramarine blue, navy blue, iron blue, cobalt blue, ultramarine blue, navy blue, sianmembl, non-metallic sannin blue, indansrembl, and cobalt blue. Examples of the purple pigment include cobalt violet, manganese violet, quinacridone violet, quinacridone red, and dioxazine violet. In addition, examples of anti-reflective ingredients include zinc dust, lead suboxide, leadtan, zinc chromate, calcium plumbate, sodium tin chromate, cyanamide lead, basic lead chromate, basic lead sulfate, MIO, etc. . Metal powder pigments are used to give a metallic feel, and include aluminum powder (aluminum flakes), bronze powder (bronze flakes), my strength, shell powder, pearl powder, and fish scales. The extender includes calcium carbonate, clay, kaolin, diatomaceous earth, silica white, bentonite, talc powder, precipitated magnesium carbonate, barium sulfate, barium carbonate and the like. Other pigments include cuprous oxide, fluorescent pigments, glass beads, litharge, mica titanium foil, and mica powder.

Dyes include direct dyes, acid dyes, basic dyes, metal-containing complex dyes, and oil-soluble dyes. As the organic pigment, azo pigments, nitroso pigments, nitro pigments, basic dye lakes, mordant dye lakes, and vat dye pigments are used as necessary.

[Resin coat]

In the recycling method, in which the resin for paint and the resin for molding have compatibility (solubility) and are pulverized and pelletized with the coating still applied, when the resin for paint is a thermoplastic resin, all of the pigments in the paint are used. A part or part of the resin is transferred into the molding resin at the stage of heating and melting at the time of regeneration (the coating film is heated and melted). As a result, the amount of incompatible (soluble) substances in the molding resin (the “pigment” dyes are poorly compatible with the molding metaphor) is increased. As a result, the physical properties of the molding resin are reduced in the coating film. It decreases after regeneration due to the effect of the pigment.

To solve the problem, the pigment is used for the purpose of giving a bond at the interface / boundary region between the molding resin and the pigment {so-called compatibility (solubility)}. A resin coating is carried out by a known method described in Japanese Patent Application Laid-Open No. Sho 644-4066, Japanese Patent Application Laid-Open No. Sho 51-111818 or Japanese Patent Publication No. Hei 11-49764. This makes it possible to reduce a decrease in the physical properties of the resin for reproduction molding. The amount of resin coat should be 0.5% by mass or more Is a necessary condition to have compatibility (solubility) with the molding resin. In addition, when aluminum flake pigment is used in a water-based paint represented by an emulsion type, the problem of corrosion of aluminum flake is solved by a resin coat.

The concept of the resin coating process will be described below using aluminum flake as an example. One type of monomer that is the same and / or similar to the molding resin for the purpose of (1) making the aluminum flake compatible with (2) the coating resin and the molding resin, preferably the molding resin to be painted. Or polymerize two or more types to grow and adsorb the resin.

This step may be repeated once or twice or more.

As long as it shows compatibility (solubility) with the molding resin and Z or the coating resin, the coating resin can be used in either thermoplastic or thermosetting. Thermosetting resins are preferred in view of the fact that they do not swell and dissolve due to heat and are not melted during the heating and melting stage during regeneration.

In the case of thermoplastic resin, the resin does not swell or dissolve in the solvent, and the melting temperature of the coat resin is higher than the temperature of heating and melting during regeneration. There is a demand not to.

When the molding resin is referred to as (A: styrene resin), thermosetting styrene-modified acrylic resin and acryl resin are suitable. Styrene-modified resin can be used, but the compatibility (solubility) is inferior to the thermosetting styrene-modified acrylic resin and acrylic resin.

(Solvent)

Solvents used in paints include normal hexane for hydrocarbons, mineral spirits containing low aromatics, toluene, xylene, terpene, methylcyclohexane, and ethylcyclohexane.For alcohols, methanol, ethanol, isopropanol, and normal butanol. Isobutanol, 2nd butyl, 3rd butyl, methyl isobutyl carbinol, etc.For ether alcohols and ethers, methyl sorb, sorb, butyl sorb, and butyl sorb, 3-methyl 3 Esters such as methoxy butanol, methyl carbitol, carbitol, butyl carbitol And ether esters, methyl acetate, ethyl acetate, isopropyl acetate, butyl acetate, isoptyl acetate, amyl acetate, methyl acetate solvent, cellosolve acetate, butylace acetate solvent, methoxybutyl acetate. Carpitol acetate, propylene glycol mono Examples of ketones such as methyl ether include acetone, methylethyl ketone, methylisobutyl ketone, cyclohexanone, diacetone alcohol, diisobutyl ketone, and isophorone.

Others include water, dimethylformamide, etc., as well as supercritical fluids, carbon dioxide, inert gases such as He, Ne, Neι, nitrogen gas, LPG, methane, ethane, propane, butane, pentane, etc. There is a liquefied gas that liquefies combustible gas, air, oxygen, chlorine, etc. (Additive)

Additives that can be used in paints include plasticizers, defoamers, anti-separation agents, anti-color unevenness agents, anti-floating agents, surfactants, anti-skinning agents, thickeners, anti-settling agents, and anti-settling agents. There are agents, anti-flow agents, anti-drip agents, preservatives, fungicides, UV stabilizers, flame retardants, antifouling agents, matting agents, stabilizers for vinyl chloride resins, antibacterial agents, etc.

(Example 1)

(Paint composition)

Aluminum pigment paste (a paste made by adding a small amount of solvent or resin to the aluminum flakes and widely used in the manufacture of paints) 10% by mass, acrylic resin varnish 1) 40% by mass , CAB resin varnish 2) 19% by mass, plasticizer

3) 2% by mass, thinner (solvent) 0¾4) 29% by mass, paint was prepared.

Here, the aluminum pigment paste has a resin coating amount of 2.5% by weight (Alpaste (trademark) FZC3080Z manufactured by Toyo Aluminum Co., Ltd.), 5.6% by weight (Alpaste (trademark) FZC6370Z) 12.4% by mass (Alpaste (trademark) FZH5660 / Toyo Aluminum), 17.1% by mass (Alpaste (trademark) FZ-U75C / Toyo Aluminum) ) And no resin coating (Alpaste (registered trademark) 110M / Toyo Aluminum, Alpaste (trademark) 7675NS / Toyo Aluminum).

The coating resin is an acrylic resin compatible with (soluble in) HiPS, and a varnish (* ^ Acrylic (trademark) A-157 (nonvolatile content: 45%) manufactured by Dainippon Ink and a normal temperature dry-type acryl resin varnish was used.

The CAB resin varnish (* 2) is manufactured using Eastman's CAB-381-0.5 cellulose acetate butylate resin (non-volatile content: 20%), and adipate ester manufactured by Dainippon Ink as a plasticizer 3). used.

Thinner (: * 4) consists of 35% by mass of ethyl acetate, 20% by mass of isopropyl alcohol, 15% by mass of isobutanol, 10% by mass of butyl acetate, and 20% by mass of butyl cellulose.

ABS resin (Technopolymer GARADE-150 TYPE- NP (natural color) Molded product 1 shown in Fig. 1 was coated on one side with the paint using the thinner and the viscosity was 11 seconds (FC # 4 / The temperature was adjusted to 20 ° C) and air-coated with a film thickness of 10. Then, it was dried in a drying oven at 50 ° C for 20 minutes to obtain a coated molded article 1 shown in Fig. 1. 2 is a rib.

〔Playback〕

The coated molded article 1 was pulverized and pelletized to obtain a recycled ABS resin pellet. Using the obtained recycled ABS pellets, a test piece (molded product) for physical property evaluation was formed and processed, and the Izod impact strength was measured and compared to confirm the effectiveness of the resin coating on the pigment. (table 1). '

(table 1)

From the viewpoint of recycling, it is desirable that the resin coating on the aluminum paste is 5% by weight or more.

(Example 2)

HI PS {Stylon 492 (trade name)} was used instead of the ABS of the first embodiment. In this case, the results were almost the same as those for ABS (Table 2).

(Table 2)

(Example 3)

In Example 3, when the modified PPE {Xyr on l O OZ (trade name)} was used, the results were almost the same as those of the ABS (Table 3).

(Table 3)

(Example 4)

When AbS {AES {unibright 70 OA (trade name)} was used, the results were almost the same as those of the ABS of Example 1 (Table 4).

(Table 4)

(Example 5)

In place of the ABS of Example 1, the result of Hi PS in which 25 parts by mass of a copolymer of styrene-grafted butyl acrylate and butadiene having PS compatibility with PS (solubility) was mixed with PS was also used. The results were almost the same as those of the ABS of Example 1 (Table 5).

(Table 5)

Flannel paste No formulation FZC6340 FZC3080 FZC6370 FZH5660 FZ-U75C 1109M 7675NS Resin coating amount

1 2.5 5.6 12.4 17.1 0 0

(Dragon%)

Izod

6.9 6.6 5.3 5.2 Impact strength 5.5 5.8 6.5 6.6

Recycling

Directivity △ 〇〇〇 XX In addition, in this example, the paint was confirmed. However, it is presumed that the present invention is also favorable in a printing ink having a similar composition to the paint.

The above-described embodiments and examples are merely examples for explanation, and the present invention is not limited thereto, but is described in the claims, the detailed description of the invention, and the drawings. Modifications and additions are possible without departing from the technical idea of the present invention that can be recognized by those skilled in the art.

For example, the present invention has described in detail a coated molded article containing a pigment in a coating film, which has been pulverized, remolded, and recycled, but the pigment coated on the surface described in the present invention is coated on the surface. It goes without saying that the same effect can be obtained when it is contained in a molded article without a coating film and remolded. '' Industrial applicability

INDUSTRIAL APPLICATION This invention can be utilized for recycling of a thermoplastic resin molded article.

Claims

The scope of the claims

1. A molded article obtained by coating at least a part of a molded article mainly composed of a thermoplastic resin with a paint mainly composed of a thermoplastic resin having compatibility (solubility) with the thermoplastic resin, As it is, the recycled thermoplastic resin molded product that has been pulverized and re-formed

A pigment is added to the paint, and the pigment is subjected to surface treatment with a resin having compatibility (solubility) with the thermoplastic resin constituting the molded article and the thermoplastic resin constituting the paint. Recycled thermoplastic resin molding

2. The recycled thermoplastic resin molded article according to claim 1, wherein the pigment is an inorganic and / or organic compound.

3. The recycled thermoplastic resin molded article according to claim 1, wherein the pigment is aluminum flake.

4. The recycled thermoplastic resin molded product according to claim 2 or 3, wherein the thermoplastic resin constituting the coating material is a thermoplastic acrylic resin or a styrene-modified acryl resin.

5. The recycled thermoplastic resin molded article according to claim 3, wherein the aluminum flake is coated with an organic polymer.

6. The recycled thermoplastic resin molded article according to claim 5, wherein the organic polymer is an acrylic resin.

7. The aluminum flakes are prepared by dissolving an ethylenically unsaturated monomer in an organic solvent and heating and polymerizing in the presence of a polymerization initiator.

Or the copolymer obtained by reacting at least two kinds selected from the group consisting of an oligomer having at least one polymerizable double bond and a monomer, according to claim 5, Recycled thermoplastic resin molded product

8. The recycled thermoplastic resin molding according to claim 5, wherein the coating amount of the organic polymer covering the aluminum flakes is 0.5% by mass or more based on the mass of the aluminum flakes. Goods